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CHEBI:42106 - L-1,4-dithiothreitol

ChEBI IDCHEBI:42106
ChEBI NameL-1,4-dithiothreitol
Stars
ASCII NameL-1,4-dithiothreitol
Secondary ChEBI IDsCHEBI:32885, CHEBI:42102
Last Modified28 July 2014
SubmitterKirill Degtyarenko
DownloadsMolfile
FormulaC4H10O2S2
Net Charge0
Average Mass154.256
Monoisotopic Mass154.01222
SMILESO[C@@H](CS)[C@@H](O)CS
InChIInChI=1S/C4H10O2S2/c5-3(1-7)4(6)2-8/h3-8H,1-2H2/t3-,4-/m0/s1
InChIKeyVHJLVAABSRFDPM-IMJSIDKUSA-N
Wikipedia
Roles Classification
Chemical Roles:
reducing agent  The element or compound in a reduction-oxidation (redox) reaction that donates an electron to another species.
chelator  A ligand with two or more separate binding sites that can bind to a single metallic central atom, forming a chelate.
Biological Role:
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
ChEBI Ontology
Outgoing Relation(s)
L-1,4-dithiothreitol (CHEBI:42106) is a 1,4-dithiothreitol (CHEBI:18320)
L-1,4-dithiothreitol (CHEBI:42106) is enantiomer of D-1,4-dithiothreitol (CHEBI:42170)
Incoming Relation(s)
D-1,4-dithiothreitol (CHEBI:42170) is enantiomer of L-1,4-dithiothreitol (CHEBI:42106)
IUPAC Name 
(2R,3R)-1,4-disulfanylbutane-2,3-diol
Synonyms  Source
2,3-DIHYDROXY-1,4-DITHIOBUTANEPDBeChem
(2R,3R)-1,4-dimercaptobutane-2,3-diolPDBeChem
L-1,4-dithiothreitolChemIDplus
L-dithiothreitolChemIDplus
L-DTTChemIDplus
L-threo-1,4-dimercapto-2,3-butanediolChemIDplus
Manual XrefsDatabases
DTTPDBeChem
DithiothreitolWikipedia
C00265KEGG COMPOUND
Registry NumbersSources
Gmelin:2859Gmelin
Beilstein:2036371Beilstein
CAS:16096-97-2ChemIDplus
CAS:3483-12-3KEGG COMPOUND